Quetiapine

NDC 68180-615 · Lupin Pharmaceuticals, Inc.

Generic nameQuetiapine

Dosage formTABLET, FILM COATED, EXTENDED RELEASE

RouteORAL

Active ingredient(s)QUETIAPINE FUMARATE

Strength300 mg/1

Pharmacologic classAtypical Antipsychotic [EPC]

Marketing categoryANDA

Packages

68180-615-07 — 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68180-615-07)

FDA lists these products with the same active ingredient.

68071-3940 — quetiapine fumarate, 68180-445 — quetiapine fumarate, 68180-446 — quetiapine fumarate, 68180-447 — quetiapine fumarate, 68180-448 — quetiapine fumarate, 68180-449 — quetiapine fumarate, 68180-450 — quetiapine fumarate, 68180-612 — Quetiapine, 68180-613 — Quetiapine, 68180-614 — Quetiapine, 68180-616 — Quetiapine, 68788-7813 — Quetiapine Fumarate, 68788-8530 — Quetiapine Fumarate, 68788-8745 — quetiapine fumarate, 68788-8746 — quetiapine fumarate, 68788-8764 — quetiapine fumarate, 68788-8778 — quetiapine fumarate, 68788-8823 — Quetiapine Fumarate, 68788-8859 — Quetiapine Fumarate, 69948-002 — Quetiapine, +323 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.